Tetralogy of Fallot

Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

Camptodactyly

The distal interphalangeal joint and/or the proximal interphalangeal joint of the fingers or toes cannot be extended to 180 degrees by either active or passive extension.

Total: 2

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PMID (PMCID)
8456824	FEMALE	Infant, Newborn
	Fryns syndrome.
	Stratton RF, Young RS, Heiman HS, Carter JM. Am J Med Genet. 1993;45(5):562-4.
	She also had a unilateral cleft lip, camptodactyly, duodenal atresia, tracheomalacia, bronchomalacia, and Tetralogy of Fallot.
1891100	FEMALE	Infant, Newborn
	Fetal akinesia deformation sequence (Pena-Shokeir phenotype) associated with acquired intrauterine brain damage.
	Lavi E, Montone KT, Rorke LB, Kliman HJ. Neurology. 1991;41(9):1467-8.
	The pathologic findings included polyhydramnios, facial anomalies, arthrogryposis, camptodactyly, pulmonary hypoplasia, and tetralogy of Fallot.